Canonical Allele Identifier: CA392323287
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48415699T>C , CM000677.2:g.48415699T>C GRCh38
NC_000015.9:g.48707896T>C , CM000677.1:g.48707896T>C GRCh37
NC_000015.8:g.46495188T>C NCBI36
NG_008805.2:g.235090A>G , LRG_778:g.235090A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*696A>G ENSP00000453958.2:n.*696A>G
ENST00000674301.2:c.*1401A>G ENSP00000501333.2:n.*1401A>G
ENST00000682158.1:n.1269A>G
ENST00000682170.1:n.2069A>G
ENST00000682767.1:n.1185A>G
ENST00000316623.10:c.7888A>G MANE Select ENSP00000325527.5:p.Lys2630Glu
ENST00000674301.1:c.3054A>G ENSP00000501333.1:n.3054A>G
ENST00000316623.9:c.7888A>G ENSP00000325527.5:p.Lys2630Glu
ENST00000559133.5:c.3257A>G
ENST00000561429.1:n.143A>G
NM_000138.4:c.7888A>G , LRG_778t1:c.7888A>G NP_000129.3:p.Lys2630Glu
NM_000138.5:c.7888A>G MANE Select NP_000129.3:p.Lys2630Glu